@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP336559.RArcrCmjdg1m5fRT5Z-n9RN6aG9coraPtcagL5nSRqEFU> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP336559.RArcrCmjdg1m5fRT5Z-n9RN6aG9coraPtcagL5nSRqEFU130_head {
  this: np:hasAssertion dgn-np:NP336559.RArcrCmjdg1m5fRT5Z-n9RN6aG9coraPtcagL5nSRqEFU130_assertion;
    np:hasProvenance dgn-np:NP336559.RArcrCmjdg1m5fRT5Z-n9RN6aG9coraPtcagL5nSRqEFU130_provenance;
    np:hasPublicationInfo dgn-np:NP336559.RArcrCmjdg1m5fRT5Z-n9RN6aG9coraPtcagL5nSRqEFU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP336559.RArcrCmjdg1m5fRT5Z-n9RN6aG9coraPtcagL5nSRqEFU130_assertion a np:Assertion .
  
  dgn-np:NP336559.RArcrCmjdg1m5fRT5Z-n9RN6aG9coraPtcagL5nSRqEFU130_provenance a np:Provenance .
  
  dgn-np:NP336559.RArcrCmjdg1m5fRT5Z-n9RN6aG9coraPtcagL5nSRqEFU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP336559.RArcrCmjdg1m5fRT5Z-n9RN6aG9coraPtcagL5nSRqEFU130_assertion {
  miriam-gene:3388 a ncit:C16612 .
  
  lld:C0000768 a ncit:C7057 .
  
  dgn-gda:DGN817d532595f51887736edd63751fd12a sio:SIO_000628 miriam-gene:3388, lld:C0000768;
    a sio:SIO_001121 .
}

dgn-np:NP336559.RArcrCmjdg1m5fRT5Z-n9RN6aG9coraPtcagL5nSRqEFU130_provenance {
  dgn-np:NP336559.RArcrCmjdg1m5fRT5Z-n9RN6aG9coraPtcagL5nSRqEFU130_assertion dcterms:description
      "[In a previous study' we showed that the ICR1 epimutation is not present in growth retarded patients with dysmorphisms not typical for SRS, but its role in the development of isolated growth restriction needed to be further elucidated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
    sio:SIO_000772 miriam-pubmed:18404973;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^xsd:date .
  
  dgn-void:source_evidence_literature a eco:ECO_0000212;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}

dgn-np:NP336559.RArcrCmjdg1m5fRT5Z-n9RN6aG9coraPtcagL5nSRqEFU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:18+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
    dcterms:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
      <http://orcid.org/0000-0002-9383-528X>, <http://orcid.org/0000-0003-0169-8159>, <http://orcid.org/0000-0003-1244-7654>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}